Gene: LINC01828 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11692700
rs11692700
LINC01829 ; LINC01828
1 1.000 0.080 2 67283245 intron variant T/C snv 2.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs79294676
rs79294676
LINC01829 ; LINC01828
2 0.925 0.080 2 67277529 intron variant G/A snv 6.4E-03 0.700 1.000 1 2017 2017